Evidence map›Paper›PMID 29370181›Full record

ArticlePloS one2018

Inferring hidden causal relations between pathway members using reduced Google matrix of directed biological networks.

José Lages, Dima L Shepelyansky, Andrei Zinovyev

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. COVID-19's Impact on International Trade.Entropy (Basel, Switzerland) · 2022
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

José LagesInstitut UTINAM, Observatoire des Sciences de l'Univers THETA, CNRS, Université de Franche-Comté, 25030 Besançon, France.ORCID 0000-0001-5965-8876
Dima L ShepelyanskyLaboratoire de Physique Théorique du CNRS, IRSAMC, Université de Toulouse, CNRS, UPS, 31062 Toulouse, France.ORCID 0000-0002-2752-0765
Andrei ZinovyevInstitut Curie, PSL Research University, Mines Paris Tech, Inserm, U900, F-75005, Paris, France.ORCID 0000-0002-9517-7284

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Signaling pathways represent parts of the global biological molecular network which connects them into a seamless whole through complex direct and indirect (hidden) crosstalk whose structure can change during development or in pathological conditions. We suggest a novel methodology, called Googlomics, for the structural analysis of directed biological networks using spectral analysis of their Google matrices, using parallels with quantum scattering theory, developed for nuclear and mesoscopic physics and quantum chaos. We introduce analytical "reduced Google matrix" method for the analysis of biological network structure. The method allows inferring hidden causal relations between the members of a signaling pathway or a functionally related group of genes. We investigate how the structure of hidden causal relations can be reprogrammed as a result of changes in the transcriptional network layer during cancerogenesis. The suggested Googlomics approach rigorously characterizes complex systemic changes in the wiring of large causal biological networks in a computationally efficient way.

Indexed as

Gene Regulatory NetworksModels, BiologicalSearch EngineAlgorithmsCausalityCell LineComputational BiologyDatabases, ProteinHumansK562 CellsModels, GeneticNeoplasm ProteinsNeoplasmsQuantum TheorySignal TransductionStochastic ProcessesNeoplasm Proteins

Identifiers

PMID29370181
PMCPMC5784915

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.